US9730444B2 - Herbicidal compositions comprising isoxaben and aminopyralid - Google Patents
Herbicidal compositions comprising isoxaben and aminopyralid Download PDFInfo
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- US9730444B2 US9730444B2 US14/201,430 US201414201430A US9730444B2 US 9730444 B2 US9730444 B2 US 9730444B2 US 201414201430 A US201414201430 A US 201414201430A US 9730444 B2 US9730444 B2 US 9730444B2
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- isoxaben
- flufenacet
- aminopyralid
- ester
- agriculturally acceptable
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- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
Definitions
- herbicidal compositions comprising (a) isoxaben, (b) aminopyralid or an agriculturally acceptable salt or ester thereof, and optionally flufenacet and diflufenican.
- Also provided are methods of controlling broadleaved weeds comprising applying a herbicidally effective amount of a combination comprising (a) isoxaben, (b) aminopyralid or an agriculturally acceptable salt or ester thereof, and optionally flufenacet and diflufenican.
- Isoxaben is the common name for N-[3-(1-ethyl-1-methylpropyl)isoxazol-5-yl]-2,6-dimethoxybenzamide.
- isoxaben is a selective herbicide that inhibits cell wall biosynthesis. It is used, for example, pre-emergence in winter and spring cereals.
- Aminopyralid is the common name for 4-amino-3,6-dichloropyridine-2-carboxylic acid. As described in The Pesticide Manual , aminopyralid is a synthetic auxin used in combination with fluoroxypyr for long-term control of annual and perennial broad-leaved weeds in grassland. The Pesticide Manual specifically identifies the salt aminopyralid-triisopropanolammonium.
- Flufenacet is the common name for N-(4-fluorophenyl)-N-(1-methylethyl)-2-[[5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl]oxy]acetamide.
- flufenacet is a systemic herbicide for which the target site may be fatty acid metabolism. It is used, for example, post-emergence in maize, wheat, and rice.
- Diflufenican is the common name for N-(2,4-difluorophenyl)-2-[3-(trifluormethyl)phenoxy]-3-pyridinecarboxamide.
- diflufenican is a selective contact and residual herbicide that blocks carotenoid biosynthesis. It is used pre- and early post-emergence in autumn-sown wheat and barley to control grass and broad-leaved weeds. It is typically used in combination with other cereal herbicides, e.g. flufenacet.
- control of or controlling undesirable vegetation means killing or preventing the vegetation, or causing some other adversely modifying effect to the vegetation e.g., deviations from natural growth or development, regulation, desiccation, retardation, and the like.
- herbicide and herbicidal active ingredient mean a compound that controls undesirable vegetation when applied in an appropriate amount.
- a herbicidally effective or vegetation controlling amount is an amount of herbicidal active ingredient the application of which controls the relevant undesirable vegetation.
- applying an herbicide or herbicidal composition means delivering it directly to the targeted vegetation or to the locus thereof or to the area where control of undesired vegetation is desired.
- Methods of application include, but are not limited to pre-emergence, post-emergence, foliar, soil, and in-water applications. Described herein are methods of controlling undesirable vegetation by applying certain herbicide combinations or compositions.
- plants and vegetation include, but are not limited to, dormant seeds, germinant seeds, emerging seedlings, plants emerging from vegetative propagules, immature vegetation, and established vegetation.
- Exemplary salts include those derived from alkali or alkaline earth metals and those derived from ammonia and amines.
- Exemplary cations include sodium, potassium, magnesium, and ammonium cations of the formula: R 1 R 2 R 3 R 4 N + wherein R 1 , R 2 , R 3 and R 4 each, independently represents hydrogen or C 1 -C 12 alkyl, C 3 -C 12 alkenyl or C 3 -C 12 alkynyl, each of which is optionally substituted by one or more hydroxy, C 1 -C 4 alkoxy, C 1 -C 4 alkylthio or phenyl groups, provided that R 1 , R 2 , R 3 and R 4 are sterically compatible.
- any two of R 1 , R 2 , R 3 and R 4 together may represent an aliphatic difunctional moiety containing one to twelve carbon atoms and up to two oxygen or sulfur atoms.
- Salts can be prepared by treatment with a metal hydroxide, such as sodium hydroxide, with an amine, such as ammonia, trimethylamine, diethanolamine, 2-methylthiopropylamine, bisallylamine, 2-butoxyethylamine, morpholine, cyclododecylamine, or benzylamine or with a tetraalkylammonium hydroxide, such as tetramethylammonium hydroxide or choline hydroxide.
- a metal hydroxide such as sodium hydroxide
- an amine such as ammonia, trimethylamine, diethanolamine, 2-methylthiopropylamine, bisallylamine, 2-butoxyethylamine, morpholine, cyclododecylamine, or benzylamine or
- esters include those derived from C 1 -C 12 alkyl, C 3 -C 12 alkenyl, C 3 -C 12 alkynyl or C 7 -C 10 aryl-substituted alkyl alcohols, such as methyl alcohol, isopropyl alcohol, 1-butanol, 2-ethylhexanol, butoxyethanol, methoxypropanol, allyl alcohol, propargyl alcohol, cyclohexanol or unsubstituted or substituted benzyl alcohols.
- Benzyl alcohols may be substituted with from 1-3 substituents independently selected from halogen, C 1 -C 4 alkyl or C 1 -C 4 alkoxy.
- Esters can be prepared by coupling of the acids with the alcohol using any number of suitable activating agents such as those used for peptide couplings such as dicyclohexylcarbodiimide (DCC) or carbonyl diimidazole (CDI); by reacting the acids with alkylating agents such as alkylhalides or alkylsulfonates in the presence of a base such as triethylamine or lithium carbonate; by reacting the corresponding acid chloride of an acid with an appropriate alcohol; by reacting the corresponding acid with an appropriate alcohol in the presence of an acid catalyst or by transesterification.
- suitable activating agents such as those used for peptide couplings such as dicyclohexylcarbodiimide (DCC) or carbonyl diimidazole (CDI)
- alkylating agents such as alkylhalides or alkylsulfonates in the presence of a base such as triethylamine or lithium carbonate
- alkylating agents such as alky
- weight ratios of mixtures are calculated using the acid equivalent weight(s) of any compounds in the mixture that are salts or esters.
- herbicidal compositions comprising (a) isoxaben and (b) aminopyralid or an agriculturally acceptable salt or ester thereof, wherein the weight ratio of active ingredients is in the range of about 20-80 of (a) to about 2.5-10 of (b). In certain embodiments the weight ratio of (a) to (b) is from 0.5 to 32. In some embodiments the herbicidal active ingredients in the composition consist of isoxaben and aminopyralid or an agriculturally acceptable salt or ester thereof, i.e., these are the only herbicidally active ingredients in the composition.
- the herbicidal composition comprises (a) isoxaben, (b) aminopyralid or an agriculturally acceptable salt or ester thereof, and (c) flufenacet, wherein the weight ratio of active ingredients is in the range 20-80 of (a) to about 2.5-10 of (b) to about 100-600 of (c). In certain embodiments the weight ratio of (a) to (b) is from 0.5 to 32, and the weight ratio of (a) to (c) is from 0.05 to 0.80. In some embodiments the herbicidal active ingredients in the composition consist of isoxaben, aminopyralid or an agriculturally acceptable salt or ester thereof, and flufenacet.
- the herbicidal composition comprises (a) isoxaben, (b) aminopyralid or an agriculturally acceptable salt or ester thereof, (c) flufenacet, and (d) diflufenican wherein the weight ratio of active ingredients is in the range 20-80 of (a) to about 2.5-10 of (b) to about 100-600 of (c) to about 50-200 of (d). In certain embodiments the weight ratio of (a) to (b) is from 0.5 to 32, the weight ratio of (a) to (c) is from 0.03 to 0.80, and the weight ratio of (a) to (d) is from 0.1 to 1.6. In some embodiments the herbicidal active ingredients in the composition consist of isoxaben, aminopyralid or an agriculturally acceptable salt or ester thereof, flufenacet, and diflufenican.
- compositions may also contain an agriculturally acceptable adjuvant or carrier.
- Also provided are methods of controlling broadleaved weeds comprising applying one of the above described compositions to the locus where control is desired.
- compositions exhibit synergy as determined by the Colby's equation. Colby, S. R. Calculation of the synergistic and antagonistic response of herbicide combinations. Weeds 1967, 15, 20-22.
- Herbicidal activity is exhibited by the compositions when they are applied directly to the plant or to the locus of the plant at any stage of growth. The effect observed depends upon the plant species to be controlled, the stage of growth of the plant, the application parameters of dilution and spray drop size, the particle size of solid components, the environmental conditions at the time of use, the specific compound employed, the specific adjuvants and carriers employed, the soil type, and the like, as well as the amount of chemical applied. These and other factors can be adjusted to promote non-selective or selective herbicidal action.
- the compositions described herein are applied to relatively immature undesirable vegetation to achieve the maximum control of weeds.
- compositions and methods provided herein are utilized to control weeds in cereal crops, including but not limited to rice, wheat, barley, tritcale, oats, rye, sorghum, corn/maize, and also in cereal crops that are tolerant to glyphosate, glufosinate, dicamba, imidazolinone, phenoxy auxin, pyridyloxy auxin, aryloxyphenoxypropionate, acetyl CoA carboxylase (ACCase), acetolactate synthase (ALS), 4-hydroxyphenyl-pyruvate dioxygenase (HPPD), protoporphyrinogen oxidase (PPO), triazine, or bromoxynil.
- cereal crops including but not limited to rice, wheat, barley, tritcale, oats, rye, sorghum, corn/maize, and also in cereal crops that are tolerant to glyphosate, glufosinate
- compositions and methods provided herein are utilized to control undesirable vegetation consisting of broadleaf weeds.
- compositions and methods provided herein are utilized to control undesirable vegetation such as chickweed ( Stellaria media (L.) Vill), and geranium ( Geranium dissectum L. ).
- the composition is applied at an application rate of from about 22.5 grams active ingredient per hectare (g ai/ha) to about 890 g ai/ha based on the total amount of active ingredients in the composition. In certain embodiments, the composition is applied at an application rate of from about 35 g ai/ha to about 350 g ai/ha based on the total amount of active ingredients in the composition.
- the isoxaben is applied at a rate from about 20 g ai/ha to about 80 g ai/ha and aminopyralid or an agriculturally acceptable salt or ester thereof is applied at a rate of from about 2.5 to about 10 grams acid equivalent per hectare (g ae/ha). In some embodiments, the isoxaben is applied at a rate of about 40 g ai/ha and aminopyralid or an agriculturally acceptable salt or ester thereof is applied at a rate of about 5 g ae/ha.
- the isoxaben is applied at a rate from about 20 g ai/ha to about 80 g ai/ha
- the aminopyralid or an agriculturally acceptable salt or ester thereof is applied at a rate of from 2.5 to 10 g ae/ha
- the flufenacet is applied at a rate from about 100 g ai/ha to about 600 g ai/ha.
- the isoxaben is applied at a rate of about 40 g ai/ha
- the aminopyralid or an agriculturally acceptable salt or ester thereof is applied at a rate of about 5 g ae/ha
- the flufenacet is applied at a rate of about 200 g ai/ha.
- the isoxaben is applied at a rate from about 20 g ai/ha to about 80 g ai/ha
- the aminopyralid or an agriculturally acceptable salt or ester thereof is applied at a rate of from 2.5 to 10 g ae/ha
- the flufenacet is applied at a rate from about 100 g ai/ha to about 600 g ai/ha
- the diflufenican is applied at a rate of from about 50 g ai/ha to about 200 g ai/ha.
- the isoxaben is applied at a rate of about 40 g ai/ha
- the aminopyralid or an agriculturally acceptable salt or ester thereof is applied at a rate of about 5 g ae/ha
- the flufenacet is applied at a rate from about 200 g ai/ha
- the diflufenican is applied at a rate of about 100 g ai/ha.
- the isoxaben is applied at a rate of about 40 g ai/ha and the flufenacet is applied at a rate of about 200 g ai/ha. In some embodiments, the isoxaben is applied at a rate from about 20 g ai/ha to about 80 g ai/ha and the flufenacet is applied at a rate from about 100 g ai/ha to about 600 g ai/ha, and the diflufenican is applied at a rate of about 50-200 g ai/ha.
- the isoxaben is applied at a rate of about 40 g ai/ha
- the flufenacet is applied at a rate of about 200 g ai/ha
- the diflufenican is applied at a rate of about 100 g ai/ha.
- the components of the mixtures described herein can be applied either separately or as part of a multipart herbicidal system.
- the active ingredients are applied simultaneously, including, e.g., in the form of a composition.
- the active ingredients are applied sequentially, e.g., within 5, 10, 15, or 30 minutes of each other; 1, 2, 3, 4, 5, 10, 12, 24, 48 hour(s) of each other, or 1 week of each other.
- the mixtures described herein can be applied in conjunction with one or more other herbicides to control a wider variety of undesirable vegetation.
- the composition can be formulated with the other herbicide or herbicides, tank-mixed with the other herbicide or herbicides or applied sequentially with the other herbicide or herbicides.
- herbicides that can be employed in conjunction with the compositions and methods described herein include, but are not limited to: 4-CPA, 4-CPB, 4-CPP, 2,4-D, 2,4-D choline salt, 2,4-D esters and amines, 2,4-DB, 3,4-DA, 3,4-DB, 2,4-DEB, 2,4-DEP, 3,4-DP, 2,3,6-TBA, 2,4,5-T, 2,4,5-TB, acetochlor, acifluorfen, aclonifen, acrolein, alachlor, allidochlor, alloxydim, allyl alcohol, alorac, ametridione, ametryn, amibuzin, amicarbazone, amidosulfuron, aminocyclopyrachlor, amiprofos-methyl, amitrole, ammonium sulfamate, anilofos, anisuron, asulam, atraton, atrazine, azafenidin, azims
- compositions and methods described herein can, further, be used in conjunction with glyphosate, glufosinate, dicamba, phenoxy auxins, pyridyloxy auxins, aryloxyphenoxypropionates, acetyl CoA carboxylase (ACCase) inhibitors, imidazolinones, acetolactate synthase (ALS) inhibitors, 4-hydroxyphenyl-pyruvate dioxygenase (HPPD) inhibitors, protoporphyrinogen oxidase (PPO) inhibitors, triazines, and bromoxynil on crops that are tolerant thereto, and on crops possessing multiple or stacked traits conferring tolerance to multiple chemistries and/or multiple modes-of-action.
- glyphosate glufosinate
- dicamba phenoxy auxins
- pyridyloxy auxins pyridyloxy auxins
- aryloxyphenoxypropionates
- compositions provided herein further comprise at least one agriculturally acceptable adjuvant or carrier.
- Suitable adjuvants or carriers should not be phytotoxic to valuable crops, particularly at the concentrations employed in applying the compositions for selective weed control in the presence of crops, and should not react chemically with herbicidal components or other composition ingredients.
- Such mixtures can be designed for application directly to weeds or their locus or can be concentrates or formulations that are normally diluted with additional carriers and adjuvants before application. They can be solids, such as, for example, dusts, granules, water-dispersible granules, or wettable powders, or liquids, such as, for example, emulsifiable concentrates, solutions, emulsions or suspensions. They can also be provided as a pre-mix or tank-mixed.
- Suitable agricultural adjuvants and carriers include, but are not limited to, crop oil concentrate; nonylphenol ethoxylate; benzylcocoalkyldimethyl quaternary ammonium salt; blend of petroleum hydrocarbon, alkyl esters, organic acid, and anionic surfactant; C 9 -C 11 alkylpolyglycoside; phosphated alcohol ethoxylate; natural primary alcohol (C 12 -C 16 ) ethoxylate; di-sec-butylphenol EO-PO block copolymer; polysiloxane-methyl cap; nonylphenol ethoxylate+urea ammonium nitrate; emulsified methylated seed oil; tridecyl alcohol (synthetic) ethoxylate (8EO); tallow amine ethoxylate (15 EO); PEG (400) dioleate-99.
- crop oil concentrate nonylphenol ethoxylate
- Liquid carriers that can be employed include water and organic solvents.
- the organic solvents include, but are not limited to, petroleum fractions or hydrocarbons such as mineral oil, aromatic solvents, paraffinic oils, and the like; vegetable oils such as soybean oil, rapeseed oil, olive oil, castor oil, sunflower seed oil, coconut oil, corn oil, cottonseed oil, linseed oil, palm oil, peanut oil, safflower oil, sesame oil, tung oil and the like; esters of the above vegetable oils; esters of monoalcohols or dihydric, trihydric, or other lower polyalcohols (4-6 hydroxy containing), such as 2-ethyl hexyl stearate, n-butyl oleate, isopropyl myristate, propylene glycol dioleate, di-octyl succinate, di-butyl adipate, di-octyl phthalate and the like; esters of mono, di and polycarbox
- organic solvents include, but are not limited to toluene, xylene, petroleum naphtha, crop oil, acetone, methyl ethyl ketone, cyclohexanone, trichloroethylene, perchloroethylene, ethyl acetate, amyl acetate, butyl acetate, propylene glycol monomethyl ether and diethylene glycol monomethyl ether, methyl alcohol, ethyl alcohol, isopropyl alcohol, amyl alcohol, ethylene glycol, propylene glycol, glycerine, N-methyl-2-pyrrolidinone, N,N-dimethyl alkylamides, dimethyl sulfoxide, liquid fertilizers and the like.
- water is the carrier for the dilution of concentrates.
- Suitable solid carriers include but are not limited to talc, pyrophyllite clay, silica, attapulgus clay, kaolin clay, kieselguhr, chalk, diatomaceous earth, lime, calcium carbonate, bentonite clay, Fuller's earth, cottonseed hulls, wheat flour, soybean flour, pumice, wood flour, walnut shell flour, lignin, cellulose, and the like.
- compositions described herein further comprise one or more surface-active agents.
- surface-active agents are employed in both solid and liquid compositions, and in certain embodiments those designed to be diluted with carrier before application.
- the surface-active agents can be anionic, cationic or nonionic in character and can be employed as emulsifying agents, wetting agents, suspending agents, or for other purposes.
- Surfactants which may also be used in the present formulations are described, inter alia, in “McCutcheon's Detergents and Emulsifiers Annual,” MC Publishing Corp., Ridgewood, N.J. , 1998 and in “Encyclopedia of Surfactants,” Vol. I-III, Chemical Publishing Co., New York, 1980-81.
- Surface-active agents include, but are not limited to salts of alkyl sulfates, such as diethanolammonium lauryl sulfate; alkylarylsulfonate salts, such as calcium dodecylbenzenesulfonate; alkylphenol-alkylene oxide addition products, such as nonylphenol-C 18 ethoxylate; alcohol-alkylene oxide addition products, such as tridecyl alcohol-C 16 ethoxylate; soaps, such as sodium stearate; alkylnaphthalene-sulfonate salts, such as sodium dibutylnaphthalenesulfonate; dialkyl esters of sulfosuccinate salts, such as sodium di(2-ethylhexyl)sulfosuccinate; sorbitol esters, such as sorbitol oleate; quaternary amines, such as lauryl trimethylammonium chloride; poly-ethylene glycol est
- these materials can be used interchangeably as an agricultural adjuvant, as a liquid carrier or as a surface active agent.
- compositions include but are not limited to compatibilizing agents, antifoam agents, sequestering agents, neutralizing agents and buffers, corrosion inhibitors, dyes, odorants, spreading agents, penetration aids, sticking agents, dispersing agents, thickening agents, freezing point depressants, antimicrobial agents, and the like.
- the compositions may also contain other compatible components, for example, other herbicides, plant growth regulants, fungicides, insecticides, and the like and can be formulated with liquid fertilizers or solid, particulate fertilizer carriers such as ammonium nitrate, urea and the like.
- the concentration of the active ingredients in the compositions described herein is from 0.0005 to 98 percent by weight. In some embodiments, the concentration is from 0.0006 to 90 percent by weight.
- the active ingredients in certain embodiments, are present in a concentration from 0.1 to 98 weight percent, and in certain embodiments, 0.5 to 90 weight percent.
- Such compositions are, in certain embodiments, diluted with an inert carrier, such as water, before application.
- the diluted compositions usually applied to weeds or the locus of weeds contain, in certain embodiments, 0.0006 to 3.0 weight percent active ingredient and in certain embodiments contain 0.01 to 0.3 weight percent.
- compositions can be applied to weeds or their locus by the use of conventional ground or aerial dusters, sprayers, and granule applicators, by addition to irrigation or paddy water, and by other conventional means known to those skilled in the art.
- Results in Table 1 are for foliar-applied compositions in small plot research experiments to evaluate the efficacy of the compositions in winter wheat.
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Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14/201,430 US9730444B2 (en) | 2013-03-08 | 2014-03-07 | Herbicidal compositions comprising isoxaben and aminopyralid |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201361775031P | 2013-03-08 | 2013-03-08 | |
| US14/201,430 US9730444B2 (en) | 2013-03-08 | 2014-03-07 | Herbicidal compositions comprising isoxaben and aminopyralid |
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| Publication Number | Publication Date |
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| US20140256550A1 US20140256550A1 (en) | 2014-09-11 |
| US9730444B2 true US9730444B2 (en) | 2017-08-15 |
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| US14/201,430 Active US9730444B2 (en) | 2013-03-08 | 2014-03-07 | Herbicidal compositions comprising isoxaben and aminopyralid |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US9730444B2 (uk) |
| EP (1) | EP2964020B1 (uk) |
| CN (1) | CN105007726B (uk) |
| AR (1) | AR095069A1 (uk) |
| AU (1) | AU2014225501B2 (uk) |
| CL (1) | CL2015002390A1 (uk) |
| ES (1) | ES2654218T3 (uk) |
| IL (1) | IL240773B (uk) |
| NZ (1) | NZ710928A (uk) |
| PT (1) | PT2964020T (uk) |
| RU (1) | RU2650555C2 (uk) |
| UA (1) | UA115691C2 (uk) |
| WO (1) | WO2014138561A1 (uk) |
| ZA (1) | ZA201506053B (uk) |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2901019A1 (en) * | 2013-03-08 | 2014-09-12 | Dow Agrosciences Llc | Herbicidal compositions comprising isoxaben and flufenacet |
| WO2018187301A1 (en) * | 2017-04-06 | 2018-10-11 | Bayer Cropscience Lp | Methods for wildfire control, invasive plant control, and residual control of invasive plants |
| CA3153003C (en) | 2018-11-29 | 2023-10-17 | Bayer Cropscience Lp | Herbicidal compositions for animal grazelands and methods for applying the same |
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2014
- 2014-03-07 UA UAA201509739A patent/UA115691C2/uk unknown
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- 2014-03-07 AR ARP140100770A patent/AR095069A1/es active IP Right Grant
- 2014-03-07 ES ES14760018.3T patent/ES2654218T3/es active Active
- 2014-03-07 US US14/201,430 patent/US9730444B2/en active Active
- 2014-03-07 RU RU2015142847A patent/RU2650555C2/ru active
- 2014-03-07 CN CN201480011843.XA patent/CN105007726B/zh active Active
- 2014-03-07 EP EP14760018.3A patent/EP2964020B1/en active Active
- 2014-03-07 WO PCT/US2014/021679 patent/WO2014138561A1/en not_active Ceased
- 2014-03-07 AU AU2014225501A patent/AU2014225501B2/en active Active
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| US4636243A (en) * | 1980-09-16 | 1987-01-13 | Eli Lilly And Company | Benzamides, compositions and agricultural method |
| WO1994007368A1 (en) | 1992-10-06 | 1994-04-14 | Shell Internationale Research Maatschappij B.V. | Herbicide mixtures |
| US6297197B1 (en) * | 2000-01-14 | 2001-10-02 | Dow Agrosciences Llc | 4-aminopicolinates and their use as herbicides |
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| US20080242546A1 (en) | 2007-03-30 | 2008-10-02 | Dow Agrosciences Llc | Synergistic herbicidal composition containing chloroacetanilides and picolinic acids |
| US20090062121A1 (en) | 2007-08-27 | 2009-03-05 | Dow Agrosciences Llc | Synergistic herbicidal composition containing certain pyridine or pyrimidine carboxylic acids and certain cereal and rice herbicides |
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| US20110118119A1 (en) | 2009-11-19 | 2011-05-19 | Bruce Spesard | Synergistic pre-emergent and post-emergent weed control compositions and methods of use thereof |
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Also Published As
| Publication number | Publication date |
|---|---|
| CN105007726A (zh) | 2015-10-28 |
| AU2014225501A1 (en) | 2015-08-27 |
| UA115691C2 (uk) | 2017-12-11 |
| PT2964020T (pt) | 2018-02-08 |
| ZA201506053B (en) | 2017-03-29 |
| CL2015002390A1 (es) | 2016-02-05 |
| EP2964020A4 (en) | 2016-08-03 |
| NZ710928A (en) | 2020-03-27 |
| IL240773A0 (en) | 2015-10-29 |
| US20140256550A1 (en) | 2014-09-11 |
| RU2650555C2 (ru) | 2018-04-16 |
| WO2014138561A1 (en) | 2014-09-12 |
| ES2654218T3 (es) | 2018-02-12 |
| EP2964020A1 (en) | 2016-01-13 |
| AR095069A1 (es) | 2015-09-16 |
| EP2964020B1 (en) | 2017-11-08 |
| IL240773B (en) | 2019-02-28 |
| AU2014225501B2 (en) | 2017-04-13 |
| CN105007726B (zh) | 2017-09-29 |
| RU2015142847A (ru) | 2017-04-13 |
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